I thought it was funny that Michael Moore was brought up. I was ahead thinking of that.
I was trying to think of what celebrity might be able to put some light on this. and that is who I thought of, lol
I wrote him back on April 1st and as of yet I have not heard back from him. But his site did say he gets many many emails and that it might take some time to get a reply.
Heres a copy of my email. maybe if someone else writes too he might see how important this is.
Paula
Date: Fri, 1 Apr 2005 11:11:45 -0800 (PST)
From: "Paula Finley" <mylkmom@yahoo.com> View Contact Details View Contact Details
Subject: Hoping you can help find answers.
To: mike@michaelmoore.com
Dear Mr. Moore,
I have always admired the way that you have stood up
for the people and fight for them when so many others
have not. You strike me as a man who is not afraid to
go against the popular vote and fight when you feel it
is for a important and just cause. You seem to
genuinly care for the people. That is why I am writing
you today.
I am hoping that after you read my letter that you
will understand why I decided to write to you. I think
that a man of your statis might be able to find some
answers and get peoples attention about this very
serious matter.
I along with many others have tried writing to the
Congress, the President, the CDC and many other people
looking for help and some answers with no luck. Most
do not even reply back.
I don't know if you know about this or not. There is
an infectious disease, with serious consequences,
being reported by people in all 50 states, as well as
15 nations. It has been labeled "Morgellons".
This has been a baffling condition characterized by
pustules, the feeling of skin crawling,lesions and the
presence of strange fibers within the lesion and
coming out of the lesion. The fibers may be blue,
black or even red. It stings and burns and is very
painful. Some people seen white threads and little
black specks of sand-like material. They have also
been desribed as parasites or worms. They are found in
there bed, on their clothes, all over the house.
The symptoms that people with this illness experience
are not merely skin symptoms. Additional symptoms
common to people in this group are chronic fatigue,
fibromyalgia, depression, and mental confusion. Many
patients who have had this illness long term are also
reporting symptoms of neurological damage. The vast
majority of people with this disease say that they are
feeling hopeless and suicidal since physicians are
unwilling or unable to help them.
Physicians are unable to determine the cause of this
illness and clearly need immediate help from
government health agencies.
As a result of people being misdiagnosed or
undiagnosed they are turning to the internet help.
They are all trying to figure out what is happening to
then and why no one is helping them. They are very
affraid. Some people are saying that it is a terrorist
attack. Others say that our Government is doing it to
us to decrease the population. Some say it's a disease
brought back from Mars with all the space trips going
on.
Everyone is very scared and they all feel ignored and
alone. They do not think that the Doctors or the
Government cares. There have even been people who
killed themselves because they could not take it any
more. Babies have this. Tons of children have it and
are being diagnosed with ADD and ADHD because they are
miserable and acting out. They just don't feel good
and no body can help them.
I feel it is very important to inform everyone about
this. This is getting bigger and bigger. I personally
know of 7 people with this in Ohio and one is my
mother. She is getting very bad. It's starting to
cause neurological damage. There are almost 2000
people registered with Morgellons Research Foundation
with it. I'm sure there a thousands more out there
that have this but never heard about this disease but
have been wondering what on earth is going on with
them. That is how my mother felt until we heard about
this Disease. She felt very alone and that she was
losing her mind.
Could you please look at few of the websites that I
have included (below) so you can see for yourself what
I am talking about and just how bad it is. I have only
included a few of them. There are many of these sites
online. They are message boards and forums that people
are going to for support and help.
I am also including the link to the Morgellons
Research Foundation, where you can find out more about
the Disease.
I feel that after you read what these people are
saying and going through that you will feel the same
way I do. That something needs to be done about this
disease and for these people as soon as possible. Also
to find out where it came from and how it started.
Thank you very much for your time and I hope that in
someway you are able to help.
Sincerely,
Paula Finley
-----------------------------------------
Morgellons Research Foundation
www.morgellons.org/Mary M. Leitao, Executive Director
Douglas Buckner, Ph.D., Associate Director
Charles E. Holman, Chairman, Board of Directors
Jeffrey S. Greene, Secretary, Board of Directors
Gregory V. Smith, M.D., Board of Directors, Medical
Advisory Board
----------------------------------------------------
You can watch a video clip of a family in Florida with
this infectious disease using the web address below.
You will note that the entire family of six is
severely affected, and the Dill children are home
schooled due to severe fatigue. You will also will
note the father, Tom Dill's, contracted and atrophied
arms, as well as his slurred speech, as he does his
interview in a wheelchair. The later stages of this
untreated infectious disease often affects people
neurologically and psychiatrically.
video.cbs47.com/viewer/viewerpage.php?Art_ID=505&tf=CBS47viewer.tpl&PreloadContract_DefID=1&Contract_DefID=2---------------------------------------------------
Message board post from people with this mystery
disease
lymebusters.proboards39.com/index.cgi?board=rash216.122.128.184/dc/dcboard.php?az=show_topics&forum=2&page=google search
www.google.com/search?q=morgellons&sourceid=mozilla-search&start=0&start=0&ie=utf-8&oe=utf-8&client=firefox-a&rls=org.mozilla:en-US:official